Melting Point and Composition Distribution of Polyolefins by Fractionation

The fractionation technique described in this paper was used to characterize the melting-point, monomer, and blocking distributions for polymers and copolymers. It is different from the molecular-weight fractionation technique in that the fractions are obtained by using a single solvent to extract the solid polymer below its melting point at stepwise-increasing temperatures. The reproducibility of this technique is excellent, and the technique is sufficient to distinguish pellet-to-pellet variation in a commercially available polypropylene. It was used to show the influence of preparation variables on the melting-point distributions of polyethylene and polypropylene and on the monomer and blocking distribution of copolymers, and to distinguish copolymers from blends.     

Comparison of visual immunoassay and chromogenic culture medium for the presence of Listeria spp. in foods

Two rapid screening methods [the TECRA Listeria Visual Immunoassay (LIS-VIS) kit, an AOAC-approved 48 h visual test, which detects Listeria through colorimetry, and BCM Listeria isolation and differentiation plating agar] were used to screen U.S. Food and Drug Administration-regulated commodities for the presence of Listeria spp. Seventy-four different food samples were screened for the presence of Listeria spp. by using both protocols. Test results for the TECRA LIS-VIA showed 66 negative samples and 1 false positive, with 4 confirmed as L. monocytogenes and 3 as L. innocua. With the BCM agar, 67 samples were negative, 4 were confirmed as L. monocytogenes, and 3 were confirmed as L. innocua. Both methods showed similar results and were effective screening tools for Listeria spp. in foods. The BCM agar method proved to be a rapid, sensitive, and excellent tool for early screening and differentiation of Listeria spp. present in foods.     

The numerical solution of the thin film flow surrounding a horizontal cylinder resulting from a vertical cylindrical jet

The numerical solution of the thin film flow surrounding a horizontal cylinder resulting from a single vertical cylindrical jet is obtained. This is effected by transforming the domain of the flow, which contains a free surface, onto a rectangular parallelepiped and using a marching strategy to solve the ensuing parabolic equations. The flow terminates at a finite distance along the cylinder, its position depending on the velocity and mass flux of the jet. A comparison with the usual two-dimensional model in which the jet is replaced by a vertical sheet shows that such a representation is valid provided the overall width of the flow is not too large. In particular, the differences in heat transfer characteristics amount to a few per cent, thus validating the use of the two-dimensional model when applied to heat exchanger tubes. A comparison with the more usual multicolumn case is also considered.     

Infrared surface modes in small NiO particles

Small particle specimens of NiO (powder and arc-produced smoke) were studied using infrared spectroscopy. Size distribution and particle configuration were established using an electron microscope. The importance of surface modes (polaritons) as well as their dependence on particle shape was established in the interpretation of the spectra. Chain formation in the smoke suggested cylinder calculations which showed the presence of both bulk and surface modes, in agreement with measurements. In both samples particle shape effects broaden the spectral features in the vicinity of the surface mode. Because of large errors in calculating surface modes from optical constants derived from a diatomic model, it was also shown that accurately measured optical constants are required in the study of the surface mode problem.     

Far-infrared absorption by collisionally interacting nitrogen and methane molecules

Quantum line shape calculations of the rototranslational enhancement spectra of nitrogen-methane gaseous mixtures are reported. The calculations are based on a recent theoretical dipole function for interacting N(2) and CH(4) molecules, which accounts for the long-range induction mechanisms: multipolar inductions and dispersion force-induced dipoles. Multipolar induction alone was often found to approximate the actual dipole surfaces of pairs of interacting linear molecules reasonably well. However, in the case of the N(2)-CH(4) pair, the absorption spectra calculated with such a dipole function still show a substantial intensity defect at the high frequencies (>250 cm(-1)) when compared to existing measurements at temperatures from 126 to 297 K, much as was previously reported.     

Two-phase channel structures based on alpha-cyclodextrin-polyethylene glycol inclusion complexes

Wide-angle X-ray scattering observations of alpha-cyclodextrin (CD)-poly(ethylene glycol) (PEG) inclusion complexes (ICs) have shown for the first time that two crystalline columnar modifications (forms I and II) are produced in the process of their formation. This was made possible by precise azimuthal X-ray diffraction scanning of oriented IC samples. Form I is characterized by CDs threaded onto PEG chains and arranged along channels in the order head-to-head/tail-to-tail, while form II is formed by unbound CDs also arranged into columns in a head-to-tail and also possibly a head-to-head/tail-to-tail manner, probably as a result of template crystallization on the form I IC crystals. It was shown that similar structural peculiarities are inherent for channel structures based on ICs obtained with PEG with a wide range of molecular weights (MWs). The characteristic feature of ICs based on PEG, especially with MW > 8000, is the presence of unbound polymer in the composition of the complex. The amount of unbound PEG was shown to rise with increasing MW of PEG, resulting in greater imperfections in the IC crystalline structure. The polyblock structure of ICs based on alpha-CD and PEG was therefore proposed.     

Properties of polarization evolution in spun fibers

We study the properties of polarization evolution in sinusoidally spun fibers. It is found that, similar to linear birefringent fibers, the evolution of the state of polarization exhibits periodicity, which can be measured by distributed measurement, such as those made with a polarization optical time domain reflectometer. The spatial period is linked with the spin parameters and fiber beat length in a simple equation. In combination with a previous finding, it is shown that the spatial period is uniquely related to spun-fiber polarization mode dispersion. This suggests that distributed fiber polarization mode dispersion can be determined throughthe measurement of the spatial period obtained in a distributed measurement.